Suleiman A. Khan

LG
h-index21
10papers
598citations
Novelty42%
AI Score31

10 Papers

5.3LGJan 30, 2023Code
Regularized Weight Aggregation in Networked Federated Learning for Glioblastoma Segmentation

Muhammad Irfan Khan, Mohammad Ayyaz Azeem, Esa Alhoniemi et al.

In federated learning (FL), the global model at the server requires an efficient mechanism for weight aggregation and a systematic strategy for collaboration selection to manage and optimize communication payload. We introduce a practical and cost-efficient method for regularized weight aggregation and propose a laborsaving technique to select collaborators per round. We illustrate the performance of our method, regularized similarity weight aggregation (RegSimAgg), on the Federated Tumor Segmentation (FeTS) 2022 challenge's federated training (weight aggregation) problem. Our scalable approach is principled, frugal, and suitable for heterogeneous non-IID collaborators. Using FeTS2021 evaluation criterion, our proposed algorithm RegSimAgg stands at 3rd position in the final rankings of FeTS2022 challenge in the weight aggregation task. Our solution is open sourced at: \url{https://github.com/dskhanirfan/FeTS2022}

2.0LGAug 1, 2023
Differential Privacy for Adaptive Weight Aggregation in Federated Tumor Segmentation

Muhammad Irfan Khan, Esa Alhoniemi, Elina Kontio et al.

Federated Learning (FL) is a distributed machine learning approach that safeguards privacy by creating an impartial global model while respecting the privacy of individual client data. However, the conventional FL method can introduce security risks when dealing with diverse client data, potentially compromising privacy and data integrity. To address these challenges, we present a differential privacy (DP) federated deep learning framework in medical image segmentation. In this paper, we extend our similarity weight aggregation (SimAgg) method to DP-SimAgg algorithm, a differentially private similarity-weighted aggregation algorithm for brain tumor segmentation in multi-modal magnetic resonance imaging (MRI). Our DP-SimAgg method not only enhances model segmentation capabilities but also provides an additional layer of privacy preservation. Extensive benchmarking and evaluation of our framework, with computational performance as a key consideration, demonstrate that DP-SimAgg enables accurate and robust brain tumor segmentation while minimizing communication costs during model training. This advancement is crucial for preserving the privacy of medical image data and safeguarding sensitive information. In conclusion, adding a differential privacy layer in the global weight aggregation phase of the federated brain tumor segmentation provides a promising solution to privacy concerns without compromising segmentation model efficacy. By leveraging DP, we ensure the protection of client data against adversarial attacks and malicious participants.

3.5IRSep 12, 2023
SAGE: Structured Attribute Value Generation for Billion-Scale Product Catalogs

Athanasios N. Nikolakopoulos, Swati Kaul, Siva Karthik Gade et al.

We introduce SAGE; a Generative LLM for inferring attribute values for products across world-wide e-Commerce catalogs. We introduce a novel formulation of the attribute-value prediction problem as a Seq2Seq summarization task, across languages, product types and target attributes. Our novel modeling approach lifts the restriction of predicting attribute values within a pre-specified set of choices, as well as, the requirement that the sought attribute values need to be explicitly mentioned in the text. SAGE can infer attribute values even when such values are mentioned implicitly using periphrastic language, or not-at-all-as is the case for common-sense defaults. Additionally, SAGE is capable of predicting whether an attribute is inapplicable for the product at hand, or non-obtainable from the available information. SAGE is the first method able to tackle all aspects of the attribute-value-prediction task as they arise in practical settings in e-Commerce catalogs. A comprehensive set of experiments demonstrates the effectiveness of the proposed approach, as well as, its superiority against state-of-the-art competing alternatives. Moreover, our experiments highlight SAGE's ability to tackle the task of predicting attribute values in zero-shot setting; thereby, opening up opportunities for significantly reducing the overall number of labeled examples required for training.

1.2QMOct 17, 2020Code
A generalized deep learning model for multi-disease Chest X-Ray diagnostics

Nabit Bajwa, Kedar Bajwa, Atif Rana et al.

We investigate the generalizability of deep convolutional neural network (CNN) on the task of disease classification from chest x-rays collected over multiple sites. We systematically train the model using datasets from three independent sites with different patient populations: National Institute of Health (NIH), Stanford University Medical Centre (CheXpert), and Shifa International Hospital (SIH). We formulate a sequential training approach and demonstrate that the model produces generalized prediction performance using held out test sets from the three sites. Our model generalizes better when trained on multiple datasets, with the CheXpert-Shifa-NET model performing significantly better (p-values < 0.05) than the models trained on individual datasets for 3 out of the 4 distinct disease classes. The code for training the model will be made available open source at: www.github.com/link-to-code at the time of publication.

4.6LGDec 28, 2024
Recommender Engine Driven Client Selection in Federated Brain Tumor Segmentation

Muhammad Irfan Khan, Elina Kontio, Suleiman A. Khan et al.

This study presents a robust and efficient client selection protocol designed to optimize the Federated Learning (FL) process for the Federated Tumor Segmentation Challenge (FeTS 2024). In the evolving landscape of FL, the judicious selection of collaborators emerges as a critical determinant for the success and efficiency of collective learning endeavors, particularly in domains requiring high precision. This work introduces a recommender engine framework based on non-negative matrix factorization (NNMF) and a hybrid aggregation approach that blends content-based and collaborative filtering. This method intelligently analyzes historical performance, expertise, and other relevant metrics to identify the most suitable collaborators. This approach not only addresses the cold start problem where new or inactive collaborators pose selection challenges due to limited data but also significantly improves the precision and efficiency of the FL process. Additionally, we propose harmonic similarity weight aggregation (HSimAgg) for adaptive aggregation of model parameters. We utilized a dataset comprising 1,251 multi-parametric magnetic resonance imaging (mpMRI) scans from individuals diagnosed with glioblastoma (GBM) for training purposes and an additional 219 mpMRI scans for external evaluations. Our federated tumor segmentation approach achieved dice scores of 0.7298, 0.7424, and 0.8218 for enhancing tumor (ET), tumor core (TC), and whole tumor (WT) segmentation tasks respectively on the external validation set. In conclusion, this research demonstrates that selecting collaborators with expertise aligned to specific tasks, like brain tumor segmentation, improves the effectiveness of FL networks.

4.6LGDec 28, 2024
Election of Collaborators via Reinforcement Learning for Federated Brain Tumor Segmentation

Muhammad Irfan Khan, Elina Kontio, Suleiman A. Khan et al.

Federated learning (FL) enables collaborative model training across decentralized datasets while preserving data privacy. However, optimally selecting participating collaborators in dynamic FL environments remains challenging. We present RL-HSimAgg, a novel reinforcement learning (RL) and similarity-weighted aggregation (simAgg) algorithm using harmonic mean to manage outlier data points. This paper proposes applying multi-armed bandit algorithms to improve collaborator selection and model generalization. By balancing exploration-exploitation trade-offs, these RL methods can promote resource-efficient training with diverse datasets. We demonstrate the effectiveness of Epsilon-greedy (EG) and upper confidence bound (UCB) algorithms for federated brain lesion segmentation. In simulation experiments on internal and external validation sets, RL-HSimAgg with UCB collaborator outperformed the EG method across all metrics, achieving higher Dice scores for Enhancing Tumor (0.7334 vs 0.6797), Tumor Core (0.7432 vs 0.6821), and Whole Tumor (0.8252 vs 0.7931) segmentation. Therefore, for the Federated Tumor Segmentation Challenge (FeTS 2024), we consider UCB as our primary client selection approach in federated Glioblastoma lesion segmentation of multi-modal MRIs. In conclusion, our research demonstrates that RL-based collaborator management, e.g. using UCB, can potentially improve model robustness and flexibility in distributed learning environments, particularly in domains like brain tumor segmentation.

17.4LGApr 8, 2020
Federated Multi-view Matrix Factorization for Personalized Recommendations

Adrian Flanagan, Were Oyomno, Alexander Grigorievskiy et al.

We introduce the federated multi-view matrix factorization method that extends the federated learning framework to matrix factorization with multiple data sources. Our method is able to learn the multi-view model without transferring the user's personal data to a central server. As far as we are aware this is the first federated model to provide recommendations using multi-view matrix factorization. The model is rigorously evaluated on three datasets on production settings. Empirical validation confirms that federated multi-view matrix factorization outperforms simpler methods that do not take into account the multi-view structure of the data, in addition, it demonstrates the usefulness of the proposed method for the challenging prediction tasks of cold-start federated recommendations.

33.5IRJan 29, 2019
Federated Collaborative Filtering for Privacy-Preserving Personalized Recommendation System

Muhammad Ammad-ud-din, Elena Ivannikova, Suleiman A. Khan et al.

The increasing interest in user privacy is leading to new privacy preserving machine learning paradigms. In the Federated Learning paradigm, a master machine learning model is distributed to user clients, the clients use their locally stored data and model for both inference and calculating model updates. The model updates are sent back and aggregated on the server to update the master model then redistributed to the clients. In this paradigm, the user data never leaves the client, greatly enhancing the user' privacy, in contrast to the traditional paradigm of collecting, storing and processing user data on a backend server beyond the user's control. In this paper we introduce, as far as we are aware, the first federated implementation of a Collaborative Filter. The federated updates to the model are based on a stochastic gradient approach. As a classical case study in machine learning, we explore a personalized recommendation system based on users' implicit feedback and demonstrate the method's applicability to both the MovieLens and an in-house dataset. Empirical validation confirms a collaborative filter can be federated without a loss of accuracy compared to a standard implementation, hence enhancing the user's privacy in a widely used recommender application while maintaining recommender performance.

4.6MLJun 11, 2016
Drug response prediction by inferring pathway-response associations with Kernelized Bayesian Matrix Factorization

Muhammad Ammad-ud-din, Suleiman A. Khan, Disha Malani et al.

A key goal of computational personalized medicine is to systematically utilize genomic and other molecular features of samples to predict drug responses for a previously unseen sample. Such predictions are valuable for developing hypotheses for selecting therapies tailored for individual patients. This is especially valuable in oncology, where molecular and genetic heterogeneity of the cells has a major impact on the response. However, the prediction task is extremely challenging, raising the need for methods that can effectively model and predict drug responses. In this study, we propose a novel formulation of multi-task matrix factorization that allows selective data integration for predicting drug responses. To solve the modeling task, we extend the state-of-the-art kernelized Bayesian matrix factorization (KBMF) method with component-wise multiple kernel learning. In addition, our approach exploits the known pathway information in a novel and biologically meaningful fashion to learn the drug response associations. Our method quantitatively outperforms the state of the art on predicting drug responses in two publicly available cancer data sets as well as on a synthetic data set. In addition, we validated our model predictions with lab experiments using an in-house cancer cell line panel. We finally show the practical applicability of the proposed method by utilizing prior knowledge to infer pathway-drug response associations, opening up the opportunity for elucidating drug action mechanisms. We demonstrate that pathway-response associations can be learned by the proposed model for the well known EGFR and MEK inhibitors.

3.8MLDec 30, 2013
Identification of structural features in chemicals associated with cancer drug response: A systematic data-driven analysis

Suleiman A Khan, Seppo Virtanen, Olli P Kallioniemi et al.

Motivation: Analysis of relationships of drug structure to biological response is key to understanding off-target and unexpected drug effects, and for developing hypotheses on how to tailor drug thera-pies. New methods are required for integrated analyses of a large number of chemical features of drugs against the corresponding genome-wide responses of multiple cell models. Results: In this paper, we present the first comprehensive multi-set analysis on how the chemical structure of drugs impacts on ge-nome-wide gene expression across several cancer cell lines (CMap database). The task is formulated as searching for drug response components across multiple cancers to reveal shared effects of drugs and the chemical features that may be responsible. The com-ponents can be computed with an extension of a very recent ap-proach called Group Factor Analysis (GFA). We identify 11 compo-nents that link the structural descriptors of drugs with specific gene expression responses observed in the three cell lines, and identify structural groups that may be responsible for the responses. Our method quantitatively outperforms the limited earlier studies on CMap and identifies both the previously reported associations and several interesting novel findings, by taking into account multiple cell lines and advanced 3D structural descriptors. The novel observations include: previously unknown similarities in the effects induced by 15-delta prostaglandin J2 and HSP90 inhibitors, which are linked to the 3D descriptors of the drugs; and the induction by simvastatin of leukemia-specific anti-inflammatory response, resem-bling the effects of corticosteroids.